{"id":11951,"date":"2026-01-16T15:37:57","date_gmt":"2026-01-16T13:37:57","guid":{"rendered":"https:\/\/www.kliinikum.ee\/geneetika\/?page_id=11951"},"modified":"2026-01-16T16:20:17","modified_gmt":"2026-01-16T14:20:17","slug":"valislaboritest-vahendatavad-molekulaardiagnostika-analuusid","status":"publish","type":"page","link":"https:\/\/www.kliinikum.ee\/geneetika\/kolleegile\/tellimislehed\/valislaboritest-vahendatavad-molekulaardiagnostika-analuusid\/","title":{"rendered":"V\u00e4lislaboritest vahendatavad molekulaardiagnostika anal\u00fc\u00fcsid"},"content":{"rendered":"\n<figure class=\"wp-block-table\"><table><tbody><tr><td>1. t\u00fc\u00fcpi fatsioskapulohumeraalne lihasd\u00fcstroofia (FSHD1) \u2013 D4Z4 kordused<\/td><td><\/td><\/tr><tr><td><i class=\"fas fa-file-invoice\"><\/i> <a href=\"https:\/\/www.kliinikum.ee\/geneetika\/wp-content\/uploads\/2026\/01\/FSHD_consent-genetic-testing-engl.pdf\" target=\"_blank\" rel=\"noreferrer noopener\">FSHD_consent-genetic-testing-engl<\/a><br><i class=\"fas fa-file-invoice\"><\/i> <a href=\"https:\/\/www.kliinikum.ee\/geneetika\/wp-content\/uploads\/2026\/01\/FSHD_order_Wurzburg.pdf\" target=\"_blank\" rel=\"noreferrer noopener\">FSHD_order_W\u00fcrzburg<\/a><br><i class=\"fas fa-file-invoice\"><\/i> <a href=\"https:\/\/www.kliinikum.ee\/geneetika\/wp-content\/uploads\/2026\/01\/FSHD_questions-21.09.2022.pdf\" target=\"_blank\" rel=\"noreferrer noopener\">FSHD_questions-21.09.2022<\/a><\/td><td>\u2022 Kood: 66618 <br>\u2022 Teostaja: Zentrum Medizinische Genetic W\u00fcrzburg (Saksamaa)<br>\u2022 Ooteaeg: 3 kuud<\/td><\/tr><tr><td>2. t\u00fc\u00fcpi m\u00fcotooniline d\u00fcstroofia (DM2) - CNBP geeni fragmentanal\u00fc\u00fcs<\/td><td><\/td><\/tr><tr><td><i class=\"fas fa-file-invoice\"><\/i> <a href=\"https:\/\/www.kliinikum.ee\/geneetika\/wp-content\/uploads\/2026\/01\/CNBP_FIMLAB_Request-Form-21.docx\" target=\"_blank\" rel=\"noreferrer noopener\">CNBP_FIMLAB_Request Form 21<\/a><\/td><td>\u2022 Kood: 66618 <br>\u2022 Teostaja: FimLab (Soome)<br>\u2022 Ooteaeg: 3 kuud<\/td><\/tr><tr><td>Hemofiilia A \u2013 F8 geeni inversioonid 1. ja 22. intronis<\/td><td><\/td><\/tr><tr><td><i class=\"fas fa-file-invoice\"><\/i> <a href=\"https:\/\/www.kliinikum.ee\/geneetika\/wp-content\/uploads\/2026\/01\/Genetics_haemophilia_predictive-test_Tartu.pdf\" target=\"_blank\" rel=\"noreferrer noopener\">Genetics_haemophilia_predictive test_Tartu<\/a><br><i class=\"fas fa-file-invoice\"><\/i> <a href=\"https:\/\/www.kliinikum.ee\/geneetika\/wp-content\/uploads\/2026\/01\/Genetics_haemophilia_screening_Tartu.pdf\" target=\"_blank\" rel=\"noreferrer noopener\">Genetics_haemophilia_screening_Tartu<\/a><br><i class=\"fas fa-file-invoice\"><\/i> <a href=\"https:\/\/www.kliinikum.ee\/geneetika\/wp-content\/uploads\/2026\/01\/Info-brev-overforing-hemofilidiagnostik-engelska.pdf\" target=\"_blank\" rel=\"noreferrer noopener\">Anal\u00fc\u00fcsi infoleht<\/a><\/td><td>\u2022 Kood: 2x66618<br>\u2022 Teostaja: Lund University (Rootsi)<br>\u2022 Ooteag: 1 kuu<\/td><\/tr><tr><td>Telomeeride pikkuse m\u00e4\u00e4ramine l\u00fcmfots\u00fc\u00fctides ja kranulots\u00fc\u00fctides (Flow-FISH)<\/td><td><\/td><\/tr><tr><td><i class=\"fas fa-file-invoice\"><\/i> <a href=\"https:\/\/www.kliinikum.ee\/geneetika\/wp-content\/uploads\/2026\/01\/Telomeerid_RepeatDx_2026.pdf\" target=\"_blank\" rel=\"noreferrer noopener\">Telomeerid_RepeatDx_2026<\/a><\/td><td>\u2022 Kood: 3x66618<br>\u2022 Teostaja: Repeat Diagnostics Inc (Saksamaa)<br>\u2022 Ooteag: 2 kuud<\/td><\/tr><tr><td>Tserebellaarse ataksia, neuropaatia ja vestibulaarse arefleksia s\u00fcndroom (CANVAS) \u2013 RFC1 geeni pentanukleotiidsed kordused<\/td><td><\/td><\/tr><tr><td><i class=\"fas fa-file-invoice\"><\/i> <a href=\"https:\/\/www.kliinikum.ee\/geneetika\/wp-content\/uploads\/2026\/01\/CNBP_FIMLAB_Request-Form-21.docx\" target=\"_blank\" rel=\"noreferrer noopener\">CANVAS_FIMLAB_Request Form 21<\/a><\/td><td>\u2022 Kood: 3x66618<br>\u2022 Teostaja: FimLab (Soome)<br>\u2022 Ooteaeg:&nbsp; 4 kuud<\/td><\/tr><\/tbody><\/table><\/figure>\n\n\n\n<p><\/p>\n","protected":false},"excerpt":{"rendered":"<p>1. t\u00fc\u00fcpi fatsioskapulohumeraalne lihasd\u00fcstroofia (FSHD1) \u2013 D4Z4 kordused FSHD_consent-genetic-testing-engl FSHD_order_W\u00fcrzburg FSHD_questions-21.09.2022 \u2022 Kood: 66618 \u2022 Teostaja: Zentrum Medizinische Genetic W\u00fcrzburg (Saksamaa)\u2022 Ooteaeg: 3 kuud 2. t\u00fc\u00fcpi m\u00fcotooniline d\u00fcstroofia (DM2) - CNBP geeni fragmentanal\u00fc\u00fcs CNBP_FIMLAB_Request Form 21 \u2022 Kood: 66618 \u2022 Teostaja: FimLab (Soome)\u2022 Ooteaeg: 3 kuud Hemofiilia A \u2013 F8 geeni inversioonid 1. ja 22. [&hellip;]<\/p>\n","protected":false},"author":30,"featured_media":0,"parent":7232,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_acf_changed":false,"_uag_custom_page_level_css":"","footnotes":""},"class_list":["post-11951","page","type-page","status-publish","hentry"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.3 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>V\u00e4lislaboritest vahendatavad molekulaardiagnostika anal\u00fc\u00fcsid - Geneetika ja personaalmeditsiini kliinik<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.kliinikum.ee\/geneetika\/kolleegile\/tellimislehed\/valislaboritest-vahendatavad-molekulaardiagnostika-analuusid\/\" \/>\n<meta property=\"og:locale\" content=\"et_EE\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"V\u00e4lislaboritest vahendatavad molekulaardiagnostika anal\u00fc\u00fcsid - Geneetika ja personaalmeditsiini kliinik\" \/>\n<meta property=\"og:description\" content=\"1. t\u00fc\u00fcpi fatsioskapulohumeraalne lihasd\u00fcstroofia (FSHD1) \u2013 D4Z4 kordused FSHD_consent-genetic-testing-engl FSHD_order_W\u00fcrzburg FSHD_questions-21.09.2022 \u2022 Kood: 66618 \u2022 Teostaja: Zentrum Medizinische Genetic W\u00fcrzburg (Saksamaa)\u2022 Ooteaeg: 3 kuud 2. t\u00fc\u00fcpi m\u00fcotooniline d\u00fcstroofia (DM2) - CNBP geeni fragmentanal\u00fc\u00fcs CNBP_FIMLAB_Request Form 21 \u2022 Kood: 66618 \u2022 Teostaja: FimLab (Soome)\u2022 Ooteaeg: 3 kuud Hemofiilia A \u2013 F8 geeni inversioonid 1. ja 22. [&hellip;]\" \/>\n<meta property=\"og:url\" content=\"https:\/\/www.kliinikum.ee\/geneetika\/kolleegile\/tellimislehed\/valislaboritest-vahendatavad-molekulaardiagnostika-analuusid\/\" \/>\n<meta property=\"og:site_name\" content=\"Geneetika ja personaalmeditsiini kliinik\" \/>\n<meta property=\"article:modified_time\" content=\"2026-01-16T14:20:17+00:00\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:label1\" content=\"Est. reading time\" \/>\n\t<meta name=\"twitter:data1\" content=\"1 minut\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\\\/\\\/schema.org\",\"@graph\":[{\"@type\":\"WebPage\",\"@id\":\"https:\\\/\\\/www.kliinikum.ee\\\/geneetika\\\/kolleegile\\\/tellimislehed\\\/valislaboritest-vahendatavad-molekulaardiagnostika-analuusid\\\/\",\"url\":\"https:\\\/\\\/www.kliinikum.ee\\\/geneetika\\\/kolleegile\\\/tellimislehed\\\/valislaboritest-vahendatavad-molekulaardiagnostika-analuusid\\\/\",\"name\":\"V\u00e4lislaboritest vahendatavad molekulaardiagnostika anal\u00fc\u00fcsid - Geneetika ja personaalmeditsiini kliinik\",\"isPartOf\":{\"@id\":\"https:\\\/\\\/www.kliinikum.ee\\\/geneetika\\\/#website\"},\"datePublished\":\"2026-01-16T13:37:57+00:00\",\"dateModified\":\"2026-01-16T14:20:17+00:00\",\"breadcrumb\":{\"@id\":\"https:\\\/\\\/www.kliinikum.ee\\\/geneetika\\\/kolleegile\\\/tellimislehed\\\/valislaboritest-vahendatavad-molekulaardiagnostika-analuusid\\\/#breadcrumb\"},\"inLanguage\":\"et\",\"potentialAction\":[{\"@type\":\"ReadAction\",\"target\":[\"https:\\\/\\\/www.kliinikum.ee\\\/geneetika\\\/kolleegile\\\/tellimislehed\\\/valislaboritest-vahendatavad-molekulaardiagnostika-analuusid\\\/\"]}]},{\"@type\":\"BreadcrumbList\",\"@id\":\"https:\\\/\\\/www.kliinikum.ee\\\/geneetika\\\/kolleegile\\\/tellimislehed\\\/valislaboritest-vahendatavad-molekulaardiagnostika-analuusid\\\/#breadcrumb\",\"itemListElement\":[{\"@type\":\"ListItem\",\"position\":1,\"name\":\"Kolleegile\",\"item\":\"https:\\\/\\\/www.kliinikum.ee\\\/geneetika\\\/kolleegile\\\/\"},{\"@type\":\"ListItem\",\"position\":2,\"name\":\"Tellimislehed\",\"item\":\"https:\\\/\\\/www.kliinikum.ee\\\/geneetika\\\/kolleegile\\\/tellimislehed\\\/\"},{\"@type\":\"ListItem\",\"position\":3,\"name\":\"V\u00e4lislaboritest vahendatavad molekulaardiagnostika anal\u00fc\u00fcsid\"}]},{\"@type\":\"WebSite\",\"@id\":\"https:\\\/\\\/www.kliinikum.ee\\\/geneetika\\\/#website\",\"url\":\"https:\\\/\\\/www.kliinikum.ee\\\/geneetika\\\/\",\"name\":\"Geneetika ja personaalmeditsiini kliinik\",\"description\":\"Hoolivus, Uuendusmeelsus, P\u00e4devus ja Usaldusv\u00e4\u00e4rsus\",\"potentialAction\":[{\"@type\":\"SearchAction\",\"target\":{\"@type\":\"EntryPoint\",\"urlTemplate\":\"https:\\\/\\\/www.kliinikum.ee\\\/geneetika\\\/?s={search_term_string}\"},\"query-input\":{\"@type\":\"PropertyValueSpecification\",\"valueRequired\":true,\"valueName\":\"search_term_string\"}}],\"inLanguage\":\"et\"}]}<\/script>\n<!-- \/ Yoast SEO plugin. -->","yoast_head_json":{"title":"V\u00e4lislaboritest vahendatavad molekulaardiagnostika anal\u00fc\u00fcsid - Geneetika ja personaalmeditsiini kliinik","robots":{"index":"index","follow":"follow","max-snippet":"max-snippet:-1","max-image-preview":"max-image-preview:large","max-video-preview":"max-video-preview:-1"},"canonical":"https:\/\/www.kliinikum.ee\/geneetika\/kolleegile\/tellimislehed\/valislaboritest-vahendatavad-molekulaardiagnostika-analuusid\/","og_locale":"et_EE","og_type":"article","og_title":"V\u00e4lislaboritest vahendatavad molekulaardiagnostika anal\u00fc\u00fcsid - Geneetika ja personaalmeditsiini kliinik","og_description":"1. t\u00fc\u00fcpi fatsioskapulohumeraalne lihasd\u00fcstroofia (FSHD1) \u2013 D4Z4 kordused FSHD_consent-genetic-testing-engl FSHD_order_W\u00fcrzburg FSHD_questions-21.09.2022 \u2022 Kood: 66618 \u2022 Teostaja: Zentrum Medizinische Genetic W\u00fcrzburg (Saksamaa)\u2022 Ooteaeg: 3 kuud 2. t\u00fc\u00fcpi m\u00fcotooniline d\u00fcstroofia (DM2) - CNBP geeni fragmentanal\u00fc\u00fcs CNBP_FIMLAB_Request Form 21 \u2022 Kood: 66618 \u2022 Teostaja: FimLab (Soome)\u2022 Ooteaeg: 3 kuud Hemofiilia A \u2013 F8 geeni inversioonid 1. ja 22. [&hellip;]","og_url":"https:\/\/www.kliinikum.ee\/geneetika\/kolleegile\/tellimislehed\/valislaboritest-vahendatavad-molekulaardiagnostika-analuusid\/","og_site_name":"Geneetika ja personaalmeditsiini kliinik","article_modified_time":"2026-01-16T14:20:17+00:00","twitter_card":"summary_large_image","twitter_misc":{"Est. reading time":"1 minut"},"schema":{"@context":"https:\/\/schema.org","@graph":[{"@type":"WebPage","@id":"https:\/\/www.kliinikum.ee\/geneetika\/kolleegile\/tellimislehed\/valislaboritest-vahendatavad-molekulaardiagnostika-analuusid\/","url":"https:\/\/www.kliinikum.ee\/geneetika\/kolleegile\/tellimislehed\/valislaboritest-vahendatavad-molekulaardiagnostika-analuusid\/","name":"V\u00e4lislaboritest vahendatavad molekulaardiagnostika anal\u00fc\u00fcsid - Geneetika ja personaalmeditsiini kliinik","isPartOf":{"@id":"https:\/\/www.kliinikum.ee\/geneetika\/#website"},"datePublished":"2026-01-16T13:37:57+00:00","dateModified":"2026-01-16T14:20:17+00:00","breadcrumb":{"@id":"https:\/\/www.kliinikum.ee\/geneetika\/kolleegile\/tellimislehed\/valislaboritest-vahendatavad-molekulaardiagnostika-analuusid\/#breadcrumb"},"inLanguage":"et","potentialAction":[{"@type":"ReadAction","target":["https:\/\/www.kliinikum.ee\/geneetika\/kolleegile\/tellimislehed\/valislaboritest-vahendatavad-molekulaardiagnostika-analuusid\/"]}]},{"@type":"BreadcrumbList","@id":"https:\/\/www.kliinikum.ee\/geneetika\/kolleegile\/tellimislehed\/valislaboritest-vahendatavad-molekulaardiagnostika-analuusid\/#breadcrumb","itemListElement":[{"@type":"ListItem","position":1,"name":"Kolleegile","item":"https:\/\/www.kliinikum.ee\/geneetika\/kolleegile\/"},{"@type":"ListItem","position":2,"name":"Tellimislehed","item":"https:\/\/www.kliinikum.ee\/geneetika\/kolleegile\/tellimislehed\/"},{"@type":"ListItem","position":3,"name":"V\u00e4lislaboritest vahendatavad molekulaardiagnostika anal\u00fc\u00fcsid"}]},{"@type":"WebSite","@id":"https:\/\/www.kliinikum.ee\/geneetika\/#website","url":"https:\/\/www.kliinikum.ee\/geneetika\/","name":"Geneetika ja personaalmeditsiini kliinik","description":"Hoolivus, Uuendusmeelsus, P\u00e4devus ja Usaldusv\u00e4\u00e4rsus","potentialAction":[{"@type":"SearchAction","target":{"@type":"EntryPoint","urlTemplate":"https:\/\/www.kliinikum.ee\/geneetika\/?s={search_term_string}"},"query-input":{"@type":"PropertyValueSpecification","valueRequired":true,"valueName":"search_term_string"}}],"inLanguage":"et"}]}},"uagb_featured_image_src":{"full":false,"thumbnail":false,"medium":false,"medium_large":false,"large":false,"1536x1536":false,"2048x2048":false},"uagb_author_info":{"display_name":"K\u00fclli Kevv\u00e4i","author_link":"https:\/\/www.kliinikum.ee\/geneetika\/author\/kyllikev\/"},"uagb_comment_info":0,"uagb_excerpt":"1. t\u00fc\u00fcpi fatsioskapulohumeraalne lihasd\u00fcstroofia (FSHD1) \u2013 D4Z4 kordused FSHD_consent-genetic-testing-engl FSHD_order_W\u00fcrzburg FSHD_questions-21.09.2022 \u2022 Kood: 66618 \u2022 Teostaja: Zentrum Medizinische Genetic W\u00fcrzburg (Saksamaa)\u2022 Ooteaeg: 3 kuud 2. t\u00fc\u00fcpi m\u00fcotooniline d\u00fcstroofia (DM2) - CNBP geeni fragmentanal\u00fc\u00fcs CNBP_FIMLAB_Request Form 21 \u2022 Kood: 66618 \u2022 Teostaja: FimLab (Soome)\u2022 Ooteaeg: 3 kuud Hemofiilia A \u2013 F8 geeni inversioonid 1. ja 22.&hellip;","_links":{"self":[{"href":"https:\/\/www.kliinikum.ee\/geneetika\/wp-json\/wp\/v2\/pages\/11951","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.kliinikum.ee\/geneetika\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/www.kliinikum.ee\/geneetika\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/www.kliinikum.ee\/geneetika\/wp-json\/wp\/v2\/users\/30"}],"replies":[{"embeddable":true,"href":"https:\/\/www.kliinikum.ee\/geneetika\/wp-json\/wp\/v2\/comments?post=11951"}],"version-history":[{"count":0,"href":"https:\/\/www.kliinikum.ee\/geneetika\/wp-json\/wp\/v2\/pages\/11951\/revisions"}],"up":[{"embeddable":true,"href":"https:\/\/www.kliinikum.ee\/geneetika\/wp-json\/wp\/v2\/pages\/7232"}],"wp:attachment":[{"href":"https:\/\/www.kliinikum.ee\/geneetika\/wp-json\/wp\/v2\/media?parent=11951"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}